A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909068



Internal ID6834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9557464..9557955hg38UCSC Ensembl
chr2:9697593..9698084hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909068
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer